EP1320387B1 - Compositions pharmaceutiques pour la liberation prolongee de peptides - Google Patents
Compositions pharmaceutiques pour la liberation prolongee de peptides Download PDFInfo
- Publication number
- EP1320387B1 EP1320387B1 EP01968868A EP01968868A EP1320387B1 EP 1320387 B1 EP1320387 B1 EP 1320387B1 EP 01968868 A EP01968868 A EP 01968868A EP 01968868 A EP01968868 A EP 01968868A EP 1320387 B1 EP1320387 B1 EP 1320387B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- ligands
- peptide
- poly
- composition
- carrier macromolecule
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
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- A61K47/61—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic macromolecular compound, e.g. an oligomeric, polymeric or dendrimeric molecule the organic macromolecular compound being a polysaccharide or a derivative thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
- A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
- A61K47/62—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being a protein, peptide or polyamino acid
- A61K47/64—Drug-peptide, drug-protein or drug-polyamino acid conjugates, i.e. the modifying agent being a peptide, protein or polyamino acid which is covalently bonded or complexed to a therapeutically active agent
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
- A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
- A61K47/62—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being a protein, peptide or polyamino acid
- A61K47/64—Drug-peptide, drug-protein or drug-polyamino acid conjugates, i.e. the modifying agent being a peptide, protein or polyamino acid which is covalently bonded or complexed to a therapeutically active agent
- A61K47/645—Polycationic or polyanionic oligopeptides, polypeptides or polyamino acids, e.g. polylysine, polyarginine, polyglutamic acid or peptide TAT
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P5/00—Drugs for disorders of the endocrine system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P5/00—Drugs for disorders of the endocrine system
- A61P5/02—Drugs for disorders of the endocrine system of the hypothalamic hormones, e.g. TRH, GnRH, CRH, GRH, somatostatin
Definitions
- Sustained release systems have been developed over the past several years based on a broad range of technologies, directed to the delivery of a wide selection of pharmaceutical agents.
- the physical formats for such systems include use of microparticles, slabs or similar macroscopic systems designed for implantation, gels and emulsions, and other preparations conceived to preserve the active agent in the delivery system for an extended period of time.
- US6054555 discloses a sustained-release composition wherein the LHRH peptide is bound to a poly(aspartic acid) or poly(glutamic acid) macromolecular carrier.
- WO 98/25642 discloses a sustained-release composition wherein a LHRH peptide is bound to an anionic macromolecule, in particular carboxymethylcellulose.
- the mechanism of release for matrix-type sustained release systems is generally understood to occur by hindered diffusion of the active agent through the carrier matrix, or by erosion of the matrix over time resulting in the liberation of the incorporated active agent. These processes are not mutually exclusive, and both mechanisms may be simultaneously active in the case of a given system.
- sustained release devices have been used for the delivery of protein pharmaceutical agents, primarily as a result of the availability of recombinant proteins which have been developed for therapeutic applications in a wide variety of pathological conditions.
- Development of such systems creates greater challenges to overcome than in the case of low molecular weight drugs and pharmaceutically active substances, since proteins inherently have only marginal conformational stability, and can frequently be susceptible to conditions or processes which result in inactivation or denaturation.
- the structural alterations in proteins leading to inactivation need not involve changes in the covalent structure of the protein, but can be entirely the consequence of a disruption of an extensive system of non-covalent interactions and/or a disruption of disulfide bonds which are responsible of the preservation of the native three dimensional structure of the protein.
- This greater lability of proteins, as compared to low molecular weight drugs and other pharmaceutically active substances, creates the need for formulations able to deliver active peptides/proteins in vivo continuously for prolonged time periods.
- the present invention provides compositions as defined in the appended claims.
- the composition comprises a water insoluble, complex comprising a pharmaceutically active peptide, and a plurality of ligands for the peptide, that allow for sustained delivery of the peptide in vivo upon administration of the complex.
- the composition of the present invention can permit continuous delivery of a peptide to a subject for prolonged periods of time, e.g., one week or one month.
- the association of the peptide and the plurality of ligands in a tight, stable complex allows for loading of high concentrations of the peptide into the composition.
- the invention features a composition which includes a plurality of peptide molecules and a plurality of ligands for the peptide, the plurality of ligands being linked; wherein the peptide and the plurality of ligands together form a water insoluble complex.
- Each of the ligands is a peptidic compound.
- the complex may be in the form of a solid ( e.g. , a paste, granules, a powder, or a lyophilizate) or the powdered form of the complex can be pulverized finely enough to form stable liquid suspensions or semi-solid dispersions.
- the plurality of ligands are linked via a carrier macromolecule .
- the plurality of ligands (or sub-combinations thereof) may be attached to the carrier macromolecule covalently, via electrostatic interactions, via hydrophobic interactions, or a combination thereof.
- the peptide is selected from the group consisting of insulin, erythropoietin (EPO), growth hormone, bradykinin, parathyroid hormone, adenocorticotrophic hormone, calcitonin, vasopressin, angiotensin, desmopressin, luteinizing hormone-releasing hormone, somatostatin, glucagon, somatomedin, oxytocin, gastrin, secretin, melanocyte stimulating hormone, beta-endorphin, enkephalin, neurotensin, thyroid releasing hormone, macrophage stimulating factor, CCR-5, growth hormone releasing factor (GRF), RGD, tumor necrosis factor (TNF), interleukins (or other cytokines) or peptide mimetics thereof.
- EPO erythropoietin
- growth hormone bradykinin
- parathyroid hormone adenocorticotrophic hormone
- calcitonin vasopressin
- vasopressin angio
- the peptide is an LHRH antagonist having the structure Ac-D-Nal-4-Cl-D-Phe-D-Pal-Ser-N-Me-Tyr-D-Asn-Leu-Lys(iPr)-Pro-D-Ala, the LHRH agonist Leuprolide having the structure pGlu-His-Trp-Ser-Tyr-D-Leu-Leu-Arg-Pro(ethylamide)-Gly, or the LHRH antagonist Cetrorelix having the structure Ac-D-Nal-4-Cl-D-Phe-D-Pal-Ser-Tyr-D-Cit-Leu-Arg-Pro-D-Ala.
- the composition provides sustained delivery of the peptide to a subject for at least one week, two weeks, three weeks, four weeks, five weeks, or more, after the composition is administered to the subject.
- the present invention features a composition which includes a peptide; a plurality of ligands for the peptide, each of the ligands being negatively or positively charged; and an ionic carrier macromolecule having an electrical charge opposite to the charge of each of the ligands; wherein the plurality of ligands are linked via the macromolecule and wherein the peptide, the plurality of ligands, and the carrier macromolecule together form a water insoluble complex.
- Each of the ligands is peptidic.
- Each of the ligands is a peptidic molecule and each of the ligands comprises an amino acid sequence bearing a net electronic charge, e.g ., a positive or a negative charge.
- each of the ligands is cationic and the carrier macromolecule is anionic e.g., an anionic polyalcohol, an anionic polysaccharide, an anionic poly-amino acid, alginic acid or a salt thereof, polyglucoronic acid or salt thereof, carrageenan, poly(acrylate), poly(methylacrylate), or starch glycolate.
- each of the ligands is anionic and the carrier macromolecule is cationic, e.g. , poly-L-lysine; poly-L-arginine; a poly(allylamine); a poly(vinylamine); a poly(ethyleneimine); an N-alkylated, poly(allylamine); an N-alkylated poly(vinylamine); an N-alkylated poly(emyleneimine); diethylaminoethyl dextran; diethylaminoethyl cellulose; or poly(d-glucosamine).
- the carrier macromolecule is cationic, e.g. , poly-L-lysine; poly-L-arginine; a poly(allylamine); a poly(vinylamine); a poly(ethyleneimine); an N-alkylated, poly(allylamine); an N-alkylated poly(vinylamine); an N-alkylated poly(emyleneimine); diethyla
- the invention features a composition which includes a peptide; a plurality of ligands for the peptide, each of the ligands being positively charged, and carboxymethylcellulose; wherein the plurality of ligands are linked via the carboxymethylcellulose and wherein the peptide, the plurality of ligands, and the carboxymethylcellulose together form a water insoluble complex.
- the invention features a method for preparing a composition.
- the water insoluble complex formed may be further sterilized by, for example, heat, gamma irradiation or electron beam irradiation.
- the water insoluble complex is formed using aseptic procedures, which can also be used as another means of sterilization.
- the invention can be used in a method for treating a subject for a condition treatable with a peptide by administering to the subject a composition which includes the peptide and a plurality of ligands for the peptide, the plurality of ligands being linked; wherein the peptide and the plurality of ligands together form a water insoluble complex.
- the composition is sterilized by, for example, irradiation (e.g. , gamma irradiation) or electron beam irradiation, prior to administration in vivo.
- compositions comprising a water insoluble, complex comprising a pharmaceutically active peptide or protein, and a plurality of ligands for the peptide, that allow for sustained delivery of the peptide in vivo upon administration of the complex.
- the advantages of the compositions of the present invention include the ability for delivery of a peptide, either systemically or locally, for prolonged periods of time ( e.g. , one month) and the ability to load high concentrations of a peptide into the composition.
- the invention features a composition which includes a peptide and a plurality of ligands for the peptide, the plurality of ligands being linked; wherein the peptide and the plurality of ligands together form a water insoluble complex.
- peptide and “protein” are used interchangeably and are intended to include compounds comprising two or more amino acid residues linked by amide bonds.
- Such compounds can be natural biomolecules, such as proteins and peptide hormones, amino acid sequence variants of a natural biomolecule, or synthetic peptides.
- the peptide includes any or all of the twenty natural L-amino acids.
- the peptide can also include one or more D-amino acid residues and/or one or more non-natural amino acid residues.
- peptides include insulin, erythropoietin (EPO), growth hormone, bradykinin, parathyroid hormone, adenocorticotrophic hormone, calcitonin, vasopressin, angiotensin, desmopressin, luteinizing hormone-releasing hormone (LHRH), somatostatin, glucagon, somatomedin, oxytocin, gastrin, secretin, melanocyte stimulating hormone, beta-endorphin, enkephalin, neurotensin, thyroid releasing hormone, macrophage stimulating factor, soluble CCR-5, tumor necrosis factor (TNF), growth hormone releasing factor (GRF), GRD, soluble TNF-9 receptor, interleukin, and other cytokines or cytokine mimetics.
- EPO erythropoietin
- growth hormone bradykinin
- parathyroid hormone adenocorticotrophic hormone
- calcitonin vasopressin
- peptide is further intended to encompass peptide analogues, peptide derivatives, and peptidomimetics that mimic the chemical structure of a peptide composed of naturally-occurring amino acids.
- peptide analogue as used herein is intended to include molecules that mimic the chemical structure of a peptide and retain the functional properties of the peptide. Examples of peptide analogues include peptides comprising one or more non-natural amino acids.
- peptide derivative as used herein is intended to include peptides in which an amino acid side chain, the peptide backbone, or the amino- or carboxyl-terminus has been derivatized ( e.g., peptidic compounds with methylated amide linkages).
- peptidomimetic as used herein is intended to include peptidic compounds in which the peptide backbone is substituted with one or more benzodiazepine molecules (see, e.g., James, G.L. et al. (1993) Science 260:1937-1942 ), "inverso" peptides in which all L-amino acids are substituted with the corresponding D-amino acids, “retro-inverso" peptides (see U.S. Patent No.
- peptide back-bone i.e ., amide bond
- modifications of the amide nitrogen, the ⁇ -carbon, amide carbonyl including modifications of the amide nitrogen, the ⁇ -carbon, amide carbonyl, complete replacement of the amide bond, extensions, deletions or backbone crosslinks.
- ⁇ indicates the absence of an amide bond.
- the structure that replaces the amide group is specified within the brackets.
- Other possible modifications include an N-alkyl (or aryl) substitution ( ⁇ [CONR]), backbone crosslinking to construct lactams and other cyclic structures, and other derivatives including C-terminal hydroxymethyl derivatives, O-modified derivatives and N-terminally modified derivatives including substituted amides such as alkylamides and hydrazides.
- pharmaceutically active peptide is intended to include a peptide that exhibits a pharmacologic activity, either in its present form or upon processing in vivo (i.e., pharmaceutically active peptides include peptides with constitutive pharmacologic activity and peptides in a "pro-drug” form that have to be metabolized or processed in some way in vivo following administration in order to exhibit pharmacologic activity).
- the term "ligand" includes a molecule which has the ability to bind to or associate with a peptide.
- the ligand is a peptidic molecule.
- the ligand may be a natural ligand for the peptide (e.g ., if the peptide is an LHRH antagonist or insulin, the ligand may be an LHRH receptor or an insulin receptor, respectively) or an artificially made ligand for the peptide, such as a fragment of a natural ligand.
- the ligands are linked indirectly. They are linked to a a carrier macromolecule, via covalent interactions, via ionic interactions, via hydrophobic interactions, or a combination thereof. Accordingly, the ligand also includes a region which will allow it to interact with another ligand or with a a carrier macromolecule.
- cross-linking agent includes any agent that can be used to link the ligands of the invention.
- Preferred cross-linking agents are heterobifunctional cross-linkers, which can be used to link proteins in a stepwise manner.
- heterobifunctional cross-linkers include succinimidyl 4-(N-maleimidomethyl) cyclohexane- 1-carboxylate (SMCC), m-Maleimidobenzoyl-N- hydroxysuccinimide ester (MBS); N-succinimidyl (4-iodoacetyl) aminobenzoate (SIAB), succinimidyl 4-(p-maleimidophenyl) butyrate (SMPB), 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride (EDC); 4-succinimidyl-oxycarbonyl-a-methyl-a-(2-pyridyldithio)-tolune (SMPT), N-succinimidyl 3-(2-pyridyldithio) propionate (SPDP), succinimidyl 6-[3-(2-pyridyldithio) propionate (SPDP), succinimid
- carrier macromolecule is intended to include any macromolecule that can be used to link the ligands of the invention.
- the macromolecule has a molecular weight of at least 5 kDa, more preferably 10 kDa.
- the carrier macromolecule may comprise a single molecular species (e.g., a single type of polymer) or two or more different molecular species (e.g. , a mixture of two or more types of polymers).
- carrier macromolecule includes anionic carrier macromolecules which are negatively charged, as well as cationic carrier macromolecules which are positively charged.
- the carrier macromolecule is selected from an anionic polyalcohol , anionic polysaccharides , poly(allylamines), poly(vinylamines), poly(ethyleneimines), N-alkylated poly(allylamines), N-alkylated poly(vinylamines) or N-alkylated poly(ethyleneimines).
- anionic carrier macromolecules include carboxymethylcellulose, algin, alginate, anionic acrylic polymers, xantham gums, sodium starch glycolate, and pharmaceutically acceptable salts thereof, as well as anionic carageenan derivatives, anionic polygalacturonic acid derivatives.
- cationic polymers include poly-L-lysine, poly-L-arginine and other polymers of basic amino acids.
- the composition provides sustained delivery of the peptide to a subject after the composition is administered to the subject.
- sustained delivery is intended to refer to continual delivery of the peptide in vivo over a period of time following administration, preferably for at least several days ( e.g ., 7, 8, 9, 10, or more days); one, two, three, or four weeks; or one, two, three, of four months.
- Sustained delivery of the peptide can be demonstrated by, for example, the continued therapeutic effect of the peptide over time (e.g ., for an LHRH analogue, sustained delivery of the analogue can be demonstrated by continued suppression of testosterone synthesis over time).
- sustained delivery of the peptide may be demonstrated by detecting the presence of the peptide or a peptide metabolite in vivo over time.
- compositions of the invention as defined in the appended claims.
- the peptide has the ability to form a water-insoluble complex with the ligand and the carrier macromolecule upon combination of the peptide and the ligand and the carrier macromolecule.
- the peptides to be used in the compositions of the present invention may be isolated from natural sources (e.g. , purified by chromatography or crystallization), may be purchased, if they are commercially available, or they may be prepared by any suitable method for peptide synthesis (stepwise or convergent), including solution-phase and solid-phase chemical synthesis, or a combination of these approaches.
- Methods for chemically synthesizing peptides are well known in the art (see, e.g., Bodansky, M. Principles of Peptide Synthesis, Springer Verlag, Berlin (1993 ) and Grant, G.A (ed.). Synthetic Peptides: A User's Guide, W.H. Freeman and Company, New York (1992 ). Automated peptide synthesizers are commercially available ( e.g. , for small molecules).
- the peptides to be used in the compositions of the present invention are produced by recombinant DNA techniques.
- the desired peptide can be expressed in bacterial cells such as E. coli, insect cells (using baculovirus expression vectors) yeast cells or mammalian cells. Suitable host cells are discussed further in Goeddel, Gene Expression Technology: Methods in Enzymology 185, Academic Press, San Diego, CA (1990 ).
- the recombinant expression vector encoding the desired peptide can be transcribed and translated in vitro, for example, using T7 promoter regulatory sequences and T7. polymerase.
- Ligands that may be used in the present invention include any peptidic molecule which is capable of binding to a peptide with a binding constant of 10mM or less.
- the ligand may be a natural ligand for the peptide or an artificially made ligand for the peptide, such as a fragment of a natural ligand, or a synthetic compound.
- the ligands of the present invention can be obtained using any of the numerous approaches in combinatorial library methods known in the art, including: biological libraries; spatially addressable parallel solid phase or solution phase libraries; synthetic library methods requiring deconvolution; the "one-bead one-compound” library method; and synthetic library methods using affinity chromatography selection.
- biological libraries are limited to peptide libraries, while the other four approaches are applicable to peptide, non-peptide oligomer or small molecule libraries of compounds ( Lam, K.S. (1997) Anticancer Drug Des. 12:145 ).
- the ligand is a peptidic compound. Accordingly, libraries comprising a multiplicity of potential peptidic ligands may be used to identify ligands that bind to a peptide of interest (i.e., the peptide to be used in the composition of the invention).
- a library comprising a multiplicity of peptidic ligands can be formed by any one of several methods known in the art. For example, in one embodiment, a multiplicity of nucleic acid molecules encoding a multiplicity of random peptidic ligands are synthesized and the nucleic acid molecules are introduced into a vector that allows for expression of the encoded peptidic ligand library.
- a library is an "external” library in which the peptidic ligand library is expressed on a surface protein of a host, such as a "phage display” library (see, e.g., Smith, G.P. (1985) Science 228:1315-1317 ; Parmley, S.F. and Smith, G.P. (1988) Gene 73:305-318 ; and Cwirla, S. et al. (1990) Proc. Natl. Acad. Sci. USA 87:6378-6382 ).
- phage display see, e.g., Smith, G.P. (1985) Science 228:1315-1317 ; Parmley, S.F. and Smith, G.P. (1988) Gene 73:305-318 ; and Cwirla, S. et al. (1990) Proc. Natl. Acad. Sci. USA 87:6378-6382 ).
- a "phage display” library is intended to refer to a library in which a multiplicity of peptidic ligands is displayed on the surface of a bacteriophage, such as a filamentous phage, preferably by fusion to a coat protein of the phage ( e.g., the pIII protein or pVIII protein of filamentous phage).
- a multiplicity of nucleic acid molecules coding for peptidic ligands is synthesized and inserted into a phage vector to provide a recombinant vector.
- Suitable vectors for construction of phage display libraries include fUSE vectors, such as fUSE1, fUSE2, fUSE3 and fUSE5 ( Smith and Scott (1993) Methods Enzymol. 217:228-257 ).
- Nucleic acid molecules can be synthesized according to methods known in the art (see, e.g ., Cormack and Struhl, (1993) Science 262:244-248 ), including automated oligonucleotide synthesis.
- the vector is introduced into a suitable host cell and the recombinant phage are extruded from the cell after a growth period. This results in a supernatant containing the recombinant phage which can then be used in screening assays with the target peptide of interest (i.e ., the peptide to be used in the compositions of the invention).
- a peptidic ligand library that may be used is a phagemid library described in, for example, U.S. Patent No. 5,925,559
- a peptidic ligand library encoded by a multiplicity of nucleic acid molecules is an "internal" library, wherein the peptidic ligand members are expressed as fusions with an internal protein of a host (i.e., a non-surface protein) by inserting the nucleic acid molecules encoding the peptidic ligands into a gene encoding the internal protein.
- the internal protein may remain intracellular or may be secreted by, or recovered from, the host.
- Examples of internal proteins with which peptidic ligand library members can be fused include thioredoxin, staphnuclease, lac repressor (LacI), GAL4 and antibodies.
- An internal library vector is preferably a plasmid vector.
- an internal library preferred to as a two-hybrid system
- a two-hybrid system see e.g ., U.S. Patent No. 5,283,173 by Field ; Zervos et al. (1993) Cell 72:223-232 ; Madura et al. (1993) J. Biol. Chem. 268:12046-12054 ; Bartel et al. (1993) Biotechniques 14:920-924 ; and Iwabuchi et al.
- nucleic acid molecules encoding a multiplicity of peptidic ligands are inserted into a plasmid encoding the DNA binding domain of GAL4 (GAL4db) such that a library of GAL4db-peptide fusion proteins are encoded by the plasmid.
- Yeast cells e.g., Saccharomyces cerevisiae YPB2 cells
- the two domains of the GAL4 transcriptional activator protein are brought into sufficient proximity as to cause transcription of a reporter gene or a phenotypic marker gene whose expression is regulated by one or more GAL4 operators.
- nucleic acid molecules encoding a multiplicity of peptidic ligands are inserted into a plasmid encoding thioredoxin such that a library of thioredoxin-peptidic ligand fusion proteins are encoded by the plasmid.
- the plasmid is introduced into a bacterial host cell where the thioredoxin-peptide fusion proteins are expressed cytoplasmically.
- the fusion proteins can be selectively released from the host cells ( e.g. , by osmotic shock or freeze-thaw procedures) and recovered for use in screening assays with the target peptide of interest ( i.e ., the peptide to be used in the compositions of the invention).
- nucleic acid molecules encoding a multiplicity of peptidic ligands are inserted into a gene encoding LacI to create a fusion gene encoding a fusion protein of LacI and the peptidic ligand library members.
- the plasmid encoding the fusion peptidic ligand library members is designed such that the fusion proteins binds to the plasmid (i.e., a plasmid encoding the LacI fusion proteins includes lac operator sequences to which LacI binds) such that the fusion proteins and the plasmids encoding them can be physically linked.
- a plasmid encoding the LacI fusion proteins includes lac operator sequences to which LacI binds
- the fusion proteins and the plasmids encoding them can be physically linked.
- the cells are lysed to liberate the fusion protein and associated DNA, and the library is screened with an immobilized target (the peptide to be used in the compositions of the invention). Fusion proteins that bind to the target are recovered and the associated DNA is reintroduced into a cells for amplification and sequencing, thus allow for determination of the peptide sequence encoded by the DNA.
- la multiplicity of peptidic ligands can be synthesized directly by standard chemical methods known in the art.
- a multiplicity of peptidic ligands can be synthesized by "split synthesis" of peptidic ligands on solid supports (see, e.g., Lam, K.S. et al. (1993) Bioorg. Med Chem. Lett. 3:419-424 ).
- Other exemplary chemical syntheses of peptidic ligand libraries include the pin method (see, e.g ., Geysen, H.M. et al.
- Peptidic ligand libraries formed by direct synthesis of the peptidic ligand library members preferably are bound to a solid support (e.g ., a bead or pin, wherein each bead or pin is linked to a single peptide moiety) to facilitate separation of peptidic ligands that bind a target (the peptide to be used in the compositions of the invention) from candidate peptidic ligands that do not bind the target.
- a solid support e.g ., a bead or pin, wherein each bead or pin is linked to a single peptide moiety
- the target peptide of interest i.e ., the peptide to be used in the compositions of the invention
- the ligand library is screened with the ligand library to identify one or more library members that bind to the peptide.
- Ligands that bind the peptide i.e ., the peptide to be used in the compositions of the invention
- Ligands that bind the peptide can be selected according to known methods, such as biopanning of an immobilized target peptide with a phage display library.
- a biotinylated target peptide is immobilized on a streptavidin-coated surface either before or after contacting the target peptide with a ligand library and unbound ligands are removed by washing.
- Ligand libraries bound to a solid support can be screened by, for example, contacting the ligands immobilized on the solid support with a labeled target peptide and detecting the labeled target peptide bound to library members or, alternatively, by releasing the ligands from the solid support and assaying the resulting solution (see, e.g ., Ohlmeyer, M.H.J. et al. (1993) Proc. Natl. Acad Sci. USA 90:10922:10926 ).
- the selected library member or members have a binding constant for binding to the target peptide of 10 mM or less, preferably about 1 mM or less, about 100 nM or less, about 10 nM or less, about 5 nM or less or about 1nM or less.
- the selected library member or members preferably comprise 30 or fewer, 20 or fewer, 15 or fewer or ten or fewer amino acid residues.
- the ligands may also be linked indirectly to a carrier macromolecule, via covalent interactions, via ionic interactions, via hydrophobic interactions, or a combination thereof. Accordingly, the ligand should also include a region which will allow it to interact with another ligand or with a cross-linking agent or a carrier macromolecule.
- the ligand may be modified such that it will be able to bind to other ligands or to carrier macromolecules or cross-linking agents.
- the ligand may be fused to an amino acid sequence bearing a net electronic charge, e.g. , a polycationic peptide, such as poly-L-lysine, or a poly-anionic peptide, such as poly-L-glutamate.
- the ligands of the present invention may be modified to contain one or more acidic or basic functional groups, such that they will be able to form pharmaceutically acceptable salts with pharmaceutically acceptable bases or acids, respectively, present on, for example, other ligands, carrier macromolecules or cross-linking agents.
- Suitable bases include a hydroxide, carbonate, or bicarbonate of a pharmaceutically acceptable metal cation, with ammonia, or with a pharmaceutically acceptable organic primary, secondary or tertiary amine.
- Representative alkali or alkaline earth salts include the lithium, sodium, potassium, calcium, magnesium, and aluminum salts and the like.
- Representative organic amines useful for the formation of base addition salts include ethylamine, diethylamine, ethylenediamine, ethanolamine, diethanolamine, and piperazine.
- the ligands of the present invention may be modified to contain biotin, such that they will be able to be cross-linked with a cross-linking agent such as avidin or streptavidin; or with another ligand containing avidin or streptavidin. It is also possible to modify the ligands of the present invention to contain avidin or streptavidin, such that they will be able to be cross-linked with a cross-linking agent such as biotin; or with another ligand containing biotin.
- Peptidic ligands of the present invention may also be linked using heterobifunctional cross-linkers, which link proteins in a stepwise manner.
- heterobifunctional cross-linkers are known in the art and described herein.
- the method includes providing a peptide and a plurality of ligands for the peptide; and combining the carrier molecul with the peptide and the plurality of ligands under conditions such that a water-insoluble complex of the peptide, the plurality of ligands, and the carrier molecule forms.
- water-insoluble complex is intended to refer to a physically and chemically stable complex that forms upon appropriate combining of a peptide and a plurality of ligands (or a peptide, a plurality of ligands, and a carrier macromolecule or a cross-linking agent) according to procedures described herein.
- This complex typically takes the form of a precipitate that is produced upon combining aqueous preparations of the peptide and the plurality of ligands (or the peptide, the plurality of ligands, and the carrier macromolecule or the cross-linking agent).
- the formation of preferred water-insoluble complexes of the invention is thought to be mediated by ( e.g ., be mediated at least in part by) ionic interactions in situations where the peptide is cationic and each of the plurality of ligands (or carrier molecule or cross-linking agent) is anionic or vice versa. Additionally the formation of a water-insoluble complex of the invention may be mediated (e.g., be mediated at least in part by) hydrophobic interactions. Still further, formation of a water-insoluble complex of the invention may be mediated (e.g., be mediated at least in part by) covalent interactions.
- a solution of the peptide and a solution of the plurality of ligands are combined until a water-insoluble complex of the peptide and the plurality of ligands precipitates out of solution.
- the pH or ionic strength of the solution may be adjusted to optimize the precipitation of the complex.
- the pH should preferably be adjusted so that it is close to the physiologic pH.
- the solutions of the peptide and the plurality of ligands are aqueous solutions.
- the peptide or the plurality of ligands are not substantially water soluble prior to combination the two, then the peptide and/or plurality of ligands can be dissolved in a water-miscible solvent, such as an alcohol ( e.g ., ethanol) prior to combining the two components of the complex.
- a water-miscible solvent such as an alcohol (e.g ., ethanol) prior to combining the two components of the complex.
- the solution of the peptide and the solution of the plurality of ligands are combined and heated until a water-insoluble complex of the peptide and the plurality of ligands precipitates out of solution.
- the amounts of peptide and plurality of ligands necessary to achieve the water-insoluble complex may vary depending upon the particular peptide and ligand used, the particular solvent(s) used and/or the procedure used to achieve the complex.
- the ligand and the peptide are combined at a ratio of, for example, 0.5:1 to 0.1:1.
- the ligand and the peptide used to form the complex are combined at a weight ratio of ligand:peptide of 0.9:1, 0.8:1, 0.7:1, 0.6:1, 0.5:1, 0.4:1, 0.3:1, 0.25:1,0.2:1,0.15:1, or 0.1:1.
- Ranges intermediate to the above recited values e.g ., 0.8:1 to 0.4:1, 0.6:1 to 0.2:1, or 0.5:1 to 0.1:1 are also intended to be part of this invention.
- ranges of values using a combination of any of the above recited values as upper and/or lower limits are intended to be included.
- the peptide content of the complex is at least 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 96Il0, 97%, or 98% by weight.
- Ranges intermediate to the above recited values e.g ., at least about 50% to about 80%, at least about 60% to about 90%, or at least about 57% to about 82%, are also intended to be part of this invention.
- ranges of values using a combination of any of the above recited values as upper and/or lower limits are intended to be included.
- the precipitate can be removed from the solution by means known in the art, such as filtration (e.g ., through a 0.45 micron nylon membrane), centrifugation and the like.
- the recovered gel or paste can then be dried (e.g ., in vacuum or in a 70 °C oven) and the solid can be milled or pulverized to a powder by means known in the art (e.g ., hammer or ball milling, or in a fluid energy mill, or grinding in mortar and pestle).
- the gel or paste can be frozen and lyophilized to dryness.
- a concentration or dilution step or adjustment of the polarity, pH, or ionic strength can be introduced prior to or during isolation of the gel or past.
- the powder, gel, or paste form of the complex can be dispersed in a carrier solution to form a liquid suspension or semi-solid dispersion suitable for injection.
- a pharmaceutical formulation of the invention is a lyophilized solid, a liquid suspension or a semi-solid dispersion.
- the powder, gel, or paste form of the complex may be compressed into tablets or spheres, or extracted or compressed into a rod or disc.
- the powder, gel, or paste form of the complex may be in a crystalline amorphous or pseudocrystalline structure, or in a clathrate-like cylinder of hydration.
- the composition of the invention is a sterile formulation.
- the complex can be sterilized, optimally by irradiation (e.g ., gamma irradiation) or electron beam sterilization.
- the method of the invention for preparing a composition as described above can further comprise sterilizing the water-insoluble complex by gamma irradiation or electron beam irradiation.
- the water-insoluble complex can be isolated using conventional sterile techniques (e.g ., using sterile starting materials and carrying out the production process aseptically).
- the water-insoluble complex is formed using aseptic procedures.
- compositions including powders, liquid suspensions, semi-solid dispersions, lyophilized solids, and sterilized forms thereof ( e.g. , by gamma irradiation), prepared according to the methods of the invention, are also encompassed by the invention.
- compositions of the invention can be used in a method for treating a subject for a condition treatable with a peptide by administering to the subject a composition which includes the peptide, the plurality of ligands for the peptide, and a carrier molecule.
- the composition is sterilized by, for example, gamma irradiation or electron beam irradiation, prior to administration in vivo.
- the term "subject” is intended to include warm-blooded animals, preferably mammals, most preferably humans.
- administering to a subject is intended to refer to dispensing, delivering or applying the compositions of the invention to a subject by any suitable route for delivery of the composition to the desired location in the subject, including delivery by either the parenteral or oral route, intramuscular injection, subcutaneous/intradermal injection, intravenous injection, buccal administration, transdermal delivery and administration by the rectal, colonic, vaginal, intranasal or respiratory tract route.
- a condition treatable with a peptide is intended to include diseases, disorders and other conditions in which administration of a peptide has a desired effect, e.g ., a therapeutically beneficial effect.
- the disease, disorder, or other condition can be a local or a systemic disease, disorder, or other condition.
- CNS disorders such as cognitive and neurodegenerative disorders, examples of which include, but are not limited to, Alzheimer's disease, dementias related to Alzheimer's disease (such as Pick's disease), Parkinson's and other Lewy diffuse body diseases, senile dementia, myasthenia gravis, Huntington's disease, Gilles de la Tourette's syndrome, multiple sclerosis, amyotrophic lateral sclerosis, progressive supranuclear palsy, epilepsy, and Jakob-Creutzfieldt disease; autonomic function disorders such as hypertension and sleep disorders, and neuropsychiatric disorders, such as depression, schizophrenia, schizoaffective disorder, korsakoff's psychosis, mania, anxiety disorders, or phobic disorders; learning or memory disorders, e.g ., amnesia or age-related memory loss, attention deficit disorder, dysthymic disorder, major depressive disorder, mania, obsessive-compulsive
- CNS central nervous system
- cardiovascular system disorders such as arteriosclerosis, ischemia reperfusion injury, restenosis, arterial inflammation, vascular wall remodeling, ventricular remodeling, rapid ventricular pacing, coronary microembolism, tachycardia, bradycardia, pressure overload, aortic bending, coronary artery ligation, vascular heart disease, atrial fibrillation, Jervell syndrome, Lange-Nielsen syndrome, long-QT syndrome, congestive heart failure, sinus node dysfunction, angina, heart failure, hypertension, atrial fibrillation, atrial flutter, dilated cardiomyopathy, idiopathic cardiomyopathy, myocardial infarction, coronary artery disease, coronary artery spasm, and arrhythmia.
- cardiovascular system disorders such as arteriosclerosis, ischemia reperfusion injury, restenosis, arterial inflammation, vascular wall remodeling, ventricular remodeling, rapid ventricular pacing, coronary microembolism, tachycardia, bradycardia, pressure overload,
- conditions treatable with a peptide also include cellular proliferation, growth, differentiation, or migration disorders such as cancer, e.g ., prostate cancer, ovarian cancer, endometriosis, uterine fibroids, breast cancer, polycystic ovary syndrome, carcinoma, sarcoma, or leukemia; benign prostatic hypertrophy; tumor angiogenesis and metastasis; skeletal dysplasia; hematopoietic and/or myeloproliferative disorders.
- cancer e.g ., prostate cancer, ovarian cancer, endometriosis, uterine fibroids, breast cancer, polycystic ovary syndrome, carcinoma, sarcoma, or leukemia
- benign prostatic hypertrophy e.g ., tumor angiogenesis and metastasis
- skeletal dysplasia hematopoietic and/or myeloproliferative disorders.
- conditions treatable with a peptide include hormonal disorders, such as type I and type II diabetes mellitus, pituitary disorders (e.g ., growth disorders), thyroid disorders (e.g ., hypothyroidism or hyperthyroidism), and reproductive or fertility disorders (e.g ., disorders which affect the organs of the reproductive system, e.g ., the prostate gland, the uterus, or the vagina; disorders which involve an imbalance in the levels of a reproductive hormone in a subject; disorders affecting the ability of a subject to reproduce; and disorders affecting secondary sex characteristic development, e.g., adrenal hyperplasia).
- hormonal disorders such as type I and type II diabetes mellitus, pituitary disorders (e.g ., growth disorders), thyroid disorders (e.g ., hypothyroidism or hyperthyroidism), and reproductive or fertility disorders (e.g ., disorders which affect the organs of the reproductive system, e.g ., the prostate gland, the uterus, or the va
- Examples of conditions treatable with a peptide further include inflammatory or immune system disorders, such as viral infection, inflammatory bowel disease, ulcerative colitis, Crohn's disease, leukocyte adhesion deficiency II syndrome, peritonitis, chronic obstructive pulmonary disease, lung inflammation, asthma, acute appendicitis, septic shock, nephritis, amyloidosis, rheumatoid arthritis, chronic bronchitis, sarcoidosis, scleroderma, lupus, polymyositis, Reiter's syndrome, psoriasis, pelvic inflammatory disease, inflammatory breast disease, orbital inflammatory disease, immune deficiency disorders (e.g., HIV, common variable immunodeficiency, congenital X-linked infantile hypogammaglobulinemia, transient hypogammaglobulinemia, selective IgA deficiency, chronic mucocutaneous candidiasis, severe combined immunodefici
- Conditions treatable with a peptide also include hematopoietic or thrombotic disorders, for example, disseminated intravascular coagulation, thromboembolic vascular disease, anemia, lymphoma, leukemia, neutrophilia, neutropenia, myeloproliferative disorders, thrombocytosis, thrombocytopenia, vonWillebrand disease, and hemophilia.
- hematopoietic or thrombotic disorders for example, disseminated intravascular coagulation, thromboembolic vascular disease, anemia, lymphoma, leukemia, neutrophilia, neutropenia, myeloproliferative disorders, thrombocytosis, thrombocytopenia, vonWillebrand disease, and hemophilia.
- Conditions treatable with a peptide further include gastrointestinal and digestive disorders, such as esophageal disorders such as atresia and fistulas, stenosis, achalasia, esophageal rings and webs, hiatal hernia, lacerations, esophagitis, diverticula, systemic sclerosis (scleroderma), varices, esophageal tumors such as squamous cell carcinomas and adenocarcinomas, stomach disorders such as diaphragmatic hernias, pyloric stenosis, dyspepsia, gastritis, acute gastric erosion and ulceration, peptic ulcers, stomach tumors such as carcinomas and sarcomas, small intestine disorders such as congenital atresia and stenosis, diverticula, Meckel's diverticulum, pancreatic rests, ischemic bowel disease, infective enterocolitis, Crohn
- conditions treatable with a peptide include labor associated conditions such as premature labor or late labor.
- compositions of the invention can be administered to the subject by any route suitable for achieving the desired therapeutic result(s), although preferred routes of administration are parenteral routes, in particular intramuscular (i.m.) injection and subcutaneous/intradermal (s.c./i.d.) injection.
- parenteral routes in particular intramuscular (i.m.) injection and subcutaneous/intradermal (s.c./i.d.) injection.
- the compositions of the invention can be administered to the subject orally.
- Other suitable parental routes include intravenous injection, buccal administration, transdermal delivery and administration by the rectal, vaginal, ophthalmic, intranasal or respiratory tract route (e.g., via inhalation, inspiration, or nebulization).
- compositions of the invention can be delivered in the form of an aerosol spray from a pressurized container or dispenser which contains a suitable propellant, e.g ., a gas such as carbon dioxide, MFA, CFC, or a nebulizer.
- a suitable propellant e.g ., a gas such as carbon dioxide, MFA, CFC, or a nebulizer.
- compositions that provides sustained delivery for weeks to months by the i.m or s.c./i.d. route may not be sustained delivery of the peptide for an equivalent length of time due to clearance of the peptide by other physiological mechanisms (i.e ., the dosage form may be cleared from the site of delivery such that prolonged therapeutic effects are not observed for time periods as long as those observed with i.m or s.c./i.d. injection).
- One or more peptides may be administered to a subject at the same or a different rate to achieve a therapeutic or diagnostic result.
- compositions of the invention When administered to a subject for therapeutic purposes, the compositions of the invention contain a therapeutically effective amount of a peptide.
- a “therapeutically effective amount” refers to an amount effective, at dosages and for periods of time necessary, to achieve the desired result.
- a therapeutically effective amount of a peptide may vary according to factors such as the disease state, age, and weight of the individual, and the ability of the peptide to elicit a desired response in the subject. Dosage regimens may be adjusted to provide the optimum therapeutic response.
- a therapeutically effective amount is also one in which any toxic or detrimental effects of the peptide are outweighed by the therapeutically beneficial effects.
- a non-limiting range for a therapeutically effective amount of a peptide is 0.001 to 15 mg/kg.
- dosage values may vary with the severity of the condition to be alleviated. It is to be further understood that for any particular subject, specific dosage regimens should be adjusted over time according to the individual need and the professional judgment of the person administering or supervising the administration of the compositions, and that dosage ranges set forth herein are exemplary only and are not intended to limit the scope or practice of the claimed composition.
- compositions of the invention may be used for diagnostic purposes.
- the compositions of the invention may be used to deliver a labeled peptide-ligand complex at a side within a subject for detection of, for example, a tumor, a thrombus, or an amyloid plaque associated with Alzheimer's Disease.
- the invention can be used to provide packaged formulations containing such complexes and syringes containing such complexes.
- the invention can be used in packaged formulations for treating a subject for a condition treatable with a peptide, e.g ., a pharmaceutically active peptide, comprising a water-insoluble complex of a peptide and a plurality of ligands and a carrier macromolecule packaged with instructions for using the water-insoluble complex for treating a subject for a condition treatable with a peptide.
- the invention can be used in a syringe having a lumen, wherein a water-insoluble complex of a peptide, a plurality of ligands and a carrier macromolecule is included in the lumen.
- the ligand is a peptide comprising a binding sequence and a charged sequence.
- the binding sequence and the charged sequence can be connected directly, for example, via a peptide bond, or indirectly, for example, via an intervening peptide sequence or a nonpeptidic linking moiety.
- the binding sequence and the charged sequence overlap, that is, the binding sequence and the charged sequence share one or more amino acid residues.
- the charged sequence can be any amino acid sequence which bears a net positive or negative charge under physiological conditions.
- the charged sequence has a net polyanionic or polycationic charge at physiological pH.
- the binding sequence comprises two or more amino acid residues, preferably three or more residues, more preferably four or more residues and, most preferably five or more residues.
- the binding sequence comprises from two to about twenty amino acid residues, more preferably from about five to about twelve residues, and, most preferably, from about five to about ten residues.
- the charged sequence preferably comprises from about two to about twenty amino acid residues, more preferably from about five to about twenty residues and most preferably from about five to about twelve residues.
- the charged sequence is a sequence which facilitates transport across cell membranes.
- a variety of cationic sequences are known to serve as intracellular transport agents. Suitable examples of such sequences include the 11 residue protein transduction domain from the human immunodeficiency virus (HIV) TAT protein and similar sequences comprising multiple arginine residues, such as are described in WO 99/29721 , WO 99/55899 and WO 99/10376 ,
- Other suitable charged sequences include poly(arginine) and poly(d-arginine) sequences.
- Further suitable peptides include those described in, for example, Derossi et al., (1994) J. Biol. Chem.
- the ligand comprising a binding sequence and a charged sequence is associated, via the binding sequence, with a protein or peptide of interest, i.e., a therapeutic protein or peptide, and, via the charged sequence, to a charged carrier macromolecule, such as a charged polymer or polyelectrolyte.
- a charged carrier macromolecule such as a charged polymer or polyelectrolyte.
- the carrier macromolecule will have, under physiological conditions, an ionic charge opposite in sign to that of the charged sequence and will interact electrostatically with the charged sequence.
- the ligand molecules and the carrier macromolecule serve to crosslink multiple protein molecules and form a complex having, at most, limited aqueous solubility under physiological conditions.
- the ligand can be a non-peptidic compound which includes a binding domain and a charged domain.
- the ligand can be any molecule which binds the protein with a sufficient binding constant.
- the charged domain can include one or more, preferably two or more, functional groups which bear an electric charge under physiological conditions, for example, anionic groups such as carboxylate, carbonate, phosphonate, sulfonate, phosphate, sulfate and sulfamate groups, and cationic groups, such as primary, secondary, tertiary and quaternary ammonium, phosphonium, sulfonium, guanidinium and iminium groups.
- the charged domain has a net polycationic or polyanionic charge under physiological conditions.
- the binding domain is non-peptidic and the charged domain is a peptide sequence, such as one of the charged sequences described above.
- the ligand is a multivalent peptidic compound.
- each ligand molecule comprises two or more binding sequences which are directly or indirectly covalently connected.
- the binding sequences can be connected via their N- or C-termini to a covalent linking group.
- the covalent linking group can be peptidic or non-peptidic.
- the linking group comprises a linear peptide sequence with one binding sequence attached to its C-terminus and another binding domain attached at its N-terminus.
- the linking group is a branched peptide sequence, such as a sequence which includes one or more amino acid residues having side chains to which an additional sequence can be connected, such as a lysine (-NH 2 ), glutamate (-C(O)OH) or aspartate (-C(O)OH) residue in which the indicated side chain functional group serves as the starting point for a branching peptide sequence.
- branched peptidic linking groups can link at least two and, preferably, three or more binding sequences.
- the linking group can also be non-peptidic, for example, non-peptidic groups derived from a non-peptidic molecule having two or more functional groups which can react with the N-terminal amino group or the C-terminal carboxylate group of two or more binding sequences.
- Suitable difunctional linking groups include NH-(CH2)n-NH-, and -C(O)-(CH2)n-C(O)-, where n is two or greater, preferably two to about twenty-four.
- Other suitable linking groups can be derived from, for example, known cross-linking agents, such as polyamines and polycarboxylic acids using methods known in the art.
- cross-linking agents include, but are not limited to, succinimidyl 4-(N-maleimidomethyl) cyclohexane- 1-carboxylate (SMCC), m-Maleimidobenzoyl-N-hydroxysuccinimide ester (MBS); N-succinimidyl (4-iodoacetyl) aminobenzoate (SIAB), succinimidyl 4-(p-maleimidophenyl) butyrate (SMPB), 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride (EDC); 4-succinimidyl-oxycarbonyl-a-methyl-a-(2-pyridyldithio)-tolune (SMPT), N-succinimidyl 3-(2-pyridyldithio) propionate (SPDP), succinimidyl 6-[3-(2-pyridyldithio) propionate] hex
- the present invention further provides a solid ionic complex comprising a therapeutically active drug having an ionic charge under physiological conditions and an ionic carrier macromolecule, as described above.
- the drug can be any compound having therapeutic or diagnostic utility which includes one or more functional groups which bear an ionic charge under physiological conditions, such as one of the groups described above.
- the drug is polycationic or polyanionic under physiological conditions.
- the drug includes one or more basic nitrogen atoms, and the carrier macromolecule is an anionic polymer, such as carboxymethylcellulose.
- the drug is a peptidic compound as defined in claim 1 of the appended claims.
- a peptide ligand to human growth hormone (hGH) is isolated by affinity screening of a peptide library, as is known in the art.
- the sequence of the ligand is determined using known methods and the ligand is synthesized with an additional ten amino acid residue cationic sequence at the N- or C-terminus of the ligand, to form a modified ligand.
- Human growth hormone and the modified ligand are combined in aqueous solution in the presence of carboxymethylcellulose, thereby precipitating a solid complex comprising hGH, the modified ligand and carboxymethylcellulose.
- the peptide ligand to hGH described in Example 1 is fused to a Gly 10 linker sequence at its amino terminus using standard peptide synthesis methods.
- the resulting Gly 10 -ligand fusion peptide is then linked to the carboxyl groups of carboxymethyl cellulose via amide bonds, using synthetic methods known in the art.
- the resulting peptide-derivatized carboxymethyl cellulose is then combined in aqueous solution with hGH, and the resulting precipitate is isolated.
- the Gly10-ligand fusion peptide described in Example 2 is coupled at its N-terminus to 1,3,5-tris(2-carboxyethyl)benzene via amide bond formation, as is known in the art.
- the resulting tris(peptide) compound is then combined in solution with hGH, resulting in precipitation of a solid, which is collected by filtration.
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Claims (19)
- Composition comprenant :(a) un peptide pharmaceutiquement actif choisi dans le groupe constitué de l'insuline, de l'érythropoïétine, de l'hormone de croissance, de la bradykinine, de l'hormone parathyroïdienne, de l'hormone adrénocorticotrophe, de la calcitonine, de la vasopressine, de l'angiotensine, de la desmopressine, de la LHRH, du Leuprolide ayant la structure pGlu-His-Trp-Ser-Tyr-D-Leu-Leu-Arg-Pro(éthylamide)-Gly, du Cetrorelix ayant la structure Ac-D-Nal-4-Cl-D-Phe-D-Pal-Ser-Tyr-D-Cit-Leu-Arg-Pro-D-Ala, de Ac-D-Nal-4-Cl-D-Phe-D-Pal-Ser-N-Me-Tyr-D-Asn-Leu-Lys(iPr)-Pro-D-Ala, de la somatostatine, du glucagon, de la somatomédine, de l'oxytocine, de la gastrine, de la sécrétine, de l'hormone de stimulation des mélanocytes, de la bêta-endorphine, de l'enképhaline, de la neurotensine, de la thyréolibérine, du facteur de stimulation des macrophages, de CCR-5, du facteur onconécrosant (TNF), du facteur de libération de l'hormone de croissance (GRF), de RGD, et de l'interleukine, et(b) une pluralité de ligands pour ledit peptide, chacun desdits ligands comprenant une séquence de liaison et une séquence chargée ;
dans laquelle ladite pluralité de ligands sont des molécules peptidiques qui possèdent la capacité de se lier au dit peptide pharmaceutiquement actif avec une constante de liaison de 10 mM ou moins et sont des ligands naturels pour le peptide ou des ligands artificiels pour le peptide ; et(c) une macromolécule vectrice ionique ayant une charge opposée à la charge desdits ligands,dans laquelle ladite macromolécule vectrice est choisie dans le groupe constitué d'un polysaccharide anionique, d'un polyalcool anionique, d'un acide polyaminé anionique, d'une poly(allylamine), d'une poly(vinylamine), d'une poly(éthylèneimine), d'une poly(allylamine) N-alkylée, d'une poly(vinylamine) N-alkylée, d'une poly(éthylèneimine) N-alkylée, et d'un polymère d'acides aminés basiques ; de poly(acrylate) ; de poly(acrylate de méthyle) ; de poly-L-lysine ; de poly-L-arginine, de diéthylaminoéthyl dextrane, de diéthylaminoéthyl cellulose et de poly(d-glucosamine) ;
dans laquelle les ligands de ladite pluralité de ligands sont liés via ladite macromolécule vectrice,
dans laquelle ledit peptide pharmaceutiquement actif, ladite pluralité de ligands, et ladite macromolécule vectrice, forment ensemble un complexe insoluble dans l'eau dont la formation est médiée au moins en partie par des interactions ioniques entre la pluralité de ligands et la macromolécule vectrice, et dans laquelle la composition permet une délivrance prolongée du peptide pharmaceutiquement actif à un sujet pendant au moins une semaine après l'administration de la composition pharmaceutique au sujet. - Composition selon la revendication 1, dans laquelle la composition permet la délivrance prolongée du peptide pharmaceutiquement actif à un sujet pendant au moins deux à quatre semaines après l'administration de la composition au sujet.
- Composition selon la revendication 1, dans laquelle la macromolécule vectrice ionique est anionique et choisie dans le groupe constitué de la carboxyméthylcellulose, de l'algine, de l'alginate, du glycolate d'amidon sodique, de la carraghénine, du poly(acrylate), et du poly(acrylate de méthyle).
- Procédé de préparation d'une composition selon la revendication 1, qui comprend :la fourniture d'un peptide pharmaceutiquement actif tel que défini dans la revendication 1, d'une pluralité de ligands pour ledit peptide, chacun desdits ligands étant tel que défini dans la revendication 1, et d'une macromolécule vectrice ionique telle que définie dans la revendication 1 ayant une charge opposée à la charge desdits ligands ; et la combinaison du peptide, de la pluralité de ligands pour le peptide, et de la macromolécule vectrice dans des conditions telles qu'un complexe insoluble dans l'eau du peptide, de la pluralité de ligands, et de la macromolécule vectrice se forme, dans lequel la formation du complexe insoluble dans l'eau est médiée au moins en partie par des interactions ioniques entre la pluralité de ligands et la macromolécule vectrice.
- Procédé selon la revendication 4, comprenant en outre la stérilisation du complexe insoluble dans l'eau par irradiation gamma ou irradiation par faisceau d'électrons.
- Procédé selon les revendications 4 ou 5, dans lequel le complexe insoluble dans l'eau est formé en utilisant des procédures aseptiques.
- Utilisation d'une composition selon la revendication 1 dans la préparation d'un médicament destiné à traiter une condition pouvant être traitée avec ledit peptide pharmaceutiquement actif chez un sujet.
- Composition selon la revendication 1, dans laquelle chacun desdits ligands comprend une première région adaptée à se lier au dit peptide et une seconde région qui a une charge négative si les ligands de la pluralité de ligands ont une charge négative ou qui a une charge positive si les ligands de la pluralité de ligands ont une charge positive, et dans laquelle la macromolécule vectrice ionique a une charge opposée à la charge de ladite seconde région dans chacun desdits ligands.
- Composition selon la revendication 1, dans laquelle chacun desdits ligands comprend une pluralité de régions adaptées à se lier au dit peptide, les régions de ladite pluralité de régions étant liées de manière covalente.
- Composition selon la revendication 9, dans laquelle les régions de ladite pluralité de régions sont liées directement ou indirectement.
- Composition selon la revendication 1, dans laquelle chacun desdits ligands a une charge positive et dans laquelle ladite macromolécule vectrice a une charge négative.
- Composition selon la revendication 1, dans laquelle chacun desdits ligands a une charge négative et dans laquelle ladite macromolécule vectrice a une charge positive.
- Composition selon la revendication 1, dans laquelle chacun desdits ligands a une charge positive et dans laquelle ladite macromolécule vectrice est la carboxyméthylcellulose.
- Composition selon la revendication 1, dans laquelle chacun desdits ligands comprend une séquence de liaison et une séquence à charge positive, et dans laquelle ladite macromolécule vectrice a une charge négative.
- Composition selon la revendication 12, dans laquelle la macromolécule vectrice est choisie dans le groupe constitué de la poly-L-lysine et la poly-L-arginine, du diéthylaminoéthyl dextrane, de la diéthylaminoéthyl cellulose et de la poly(d-glucosamine).
- Composition selon la revendication 14, dans laquelle la séquence à charge positive est une poly(arginine).
- Composition selon la revendication 14, dans laquelle la séquence à charge positive est une poly(d-arginine).
- Composition selon la revendication 1, dans laquelle chacun desdits ligands comprend une séquence d'acides aminés portant une charge électronique nette qui est une poly(lysine).
- Composition selon la revendication 1, dans laquelle chacun desdits ligands comprend une séquence d'acides aminés portant une charge électronique nette qui est un poly(L-glutamate).
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US23218800P | 2000-09-13 | 2000-09-13 | |
US232188P | 2000-09-13 | ||
PCT/US2001/028691 WO2002022154A2 (fr) | 2000-09-13 | 2001-09-13 | Compositions pharmaceutiques pour medicaments a liberation prolongee |
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US (2) | US7037889B2 (fr) |
EP (1) | EP1320387B1 (fr) |
JP (1) | JP2004508411A (fr) |
AT (1) | ATE552859T1 (fr) |
AU (1) | AU2001289079A1 (fr) |
DK (1) | DK1320387T3 (fr) |
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US7494669B2 (en) * | 2001-02-28 | 2009-02-24 | Carrington Laboratories, Inc. | Delivery of physiological agents with in-situ gels comprising anionic polysaccharides |
EP1408876A4 (fr) | 2001-06-22 | 2004-09-22 | Durect Corp | Implants coaxiaux a liberation prolongee d'ordre 0 |
WO2003086382A1 (fr) * | 2002-04-11 | 2003-10-23 | Children's Medical Center Corporation | Conjugues de polymeres tnp-470 et utilisation de ceux-ci |
JP2006506321A (ja) * | 2002-04-11 | 2006-02-23 | チルドレンズ メディカル センター コーポレーション | 血管透過性亢進を阻害する方法 |
WO2004060387A1 (fr) | 2002-12-27 | 2004-07-22 | Diobex, Inc. | Compositions et procedes de prevention et reduction de l'hypoglycemie induite par l'insuline |
US7655618B2 (en) | 2002-12-27 | 2010-02-02 | Diobex, Inc. | Compositions and methods for the prevention and control of insulin-induced hypoglycemia |
MXPA05007182A (es) * | 2002-12-31 | 2006-04-07 | Altus Pharmaceuticals Inc | Complejos de cristales de proteina y polimeros ionicos. |
AU2003303646B2 (en) | 2002-12-31 | 2010-03-04 | Altus Pharmaceuticals Inc. | Human growth hormone crystals and methods for preparing them |
US20040224024A1 (en) * | 2003-04-23 | 2004-11-11 | Massachusetts Institute Of Technology | Controlled drug release formulations containing polyion complexes |
US20060193825A1 (en) * | 2003-04-29 | 2006-08-31 | Praecis Phamaceuticals, Inc. | Pharmaceutical formulations for sustained drug delivery |
JP2007525507A (ja) * | 2004-02-26 | 2007-09-06 | ザ ペン ステイト リサーチ ファンデーション | オピオイド増殖因子レセプターを用いる、新生物の処置のための組み合わせ療法 |
EP1737482A4 (fr) * | 2004-03-01 | 2010-09-15 | Lumen Therapeutics Llc | Compositions et methodes de traitement de maladies |
US8128952B2 (en) * | 2005-01-12 | 2012-03-06 | Clemson University Research Foundation | Ligand-mediated controlled drug delivery |
WO2007021970A2 (fr) * | 2005-08-15 | 2007-02-22 | Praecis Pharmaceuticals, Inc. | Formes pharmaceutiques stables et methodes d'utilisation de celles-ci |
CA2634053A1 (fr) * | 2005-12-23 | 2007-07-05 | Altus Pharmaceuticals Inc. | Compositions comprenant des cristaux de proteines complexes par des polycations et procede de traitement associe |
US7640223B2 (en) * | 2006-11-16 | 2009-12-29 | University Of Tennessee Research Foundation | Method of organizing and presenting data in a table using stutter peak rule |
JP5305371B2 (ja) * | 2007-07-19 | 2013-10-02 | 国立大学法人 岡山大学 | 生物膜透過性組成物及び薬剤の生物膜透過性増強方法 |
MX2011004082A (es) | 2008-10-17 | 2011-10-14 | Dana Farber Cancer Inst Inc | Peptidos de dominio citoplasmico muc-1 como inhibidores del cancer. |
JP5542687B2 (ja) | 2008-11-05 | 2014-07-09 | 国立大学法人 東京医科歯科大学 | ヒアルロン酸誘導体、およびその医薬組成物 |
US8614186B2 (en) * | 2009-05-27 | 2013-12-24 | Dana-Farber Cancer Institute, Inc. | Inhibition of inflammation using antagonists of MUC1 |
WO2011100688A1 (fr) | 2010-02-12 | 2011-08-18 | Dana-Farber Cancer Institute, Inc. | Antagonistes améliorés du muc1 |
US9044421B2 (en) | 2012-03-28 | 2015-06-02 | Genus Oncology, Llc | Treating MUC1-expressing cancers with combination therapies |
CN104603156B (zh) | 2012-09-05 | 2016-10-26 | 中外制药株式会社 | 引入有氨基酸和甾基的透明质酸衍生物 |
US11512147B2 (en) | 2017-11-15 | 2022-11-29 | Chugai Seiyaku Kabushiki Kaisha | Hyaluronic acid derivative modified with polyethylene glycol |
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- 2001-09-13 EP EP01968868A patent/EP1320387B1/fr not_active Expired - Lifetime
- 2001-09-13 US US09/953,247 patent/US7037889B2/en not_active Expired - Fee Related
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- 2001-09-13 JP JP2002526404A patent/JP2004508411A/ja active Pending
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Also Published As
Publication number | Publication date |
---|---|
DK1320387T3 (da) | 2012-07-16 |
US20060094662A1 (en) | 2006-05-04 |
JP2004508411A (ja) | 2004-03-18 |
US7037889B2 (en) | 2006-05-02 |
AU2001289079A1 (en) | 2002-03-26 |
WO2002022154A3 (fr) | 2003-03-13 |
US8084419B2 (en) | 2011-12-27 |
WO2002022154A2 (fr) | 2002-03-21 |
EP1320387A2 (fr) | 2003-06-25 |
US20020086829A1 (en) | 2002-07-04 |
ATE552859T1 (de) | 2012-04-15 |
ES2387537T3 (es) | 2012-09-25 |
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